Skip to main content
Canadian Medical Association Journal logoLink to Canadian Medical Association Journal
. 1969 Aug 23;101(4):185–190.

The newborn phenylketonuria screening program in Ontario.

PMCID: PMC1946107  PMID: 5811698

Full text

PDF
185

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. AUERBACH V. H., DIGEORGE A. M., BRIGHAM M. P., DOBBS J. M. Delayed maturation of tyrosine metabolism in a full-term sibling of a child with phenylketonuria. J Pediatr. 1963 Jun;62:938–940. doi: 10.1016/s0022-3476(63)80113-4. [DOI] [PubMed] [Google Scholar]
  2. Avery M. E., Clow C. L., Menkes J. H., Ramos A., Scriver C. R., Stern L., Wasserman B. P. Transient tyrosinemia of the newborn: dietary and clinical aspects. Pediatrics. 1967 Mar;39(3):378–384. [PubMed] [Google Scholar]
  3. KLEINMAN D. S. PHENYLKETONURIA. A REVIEW OF SOME DEFICITS IN OUR INFORMATION. Pediatrics. 1964 Jan;33:123–134. [PubMed] [Google Scholar]
  4. PARTINGTON M. W., ANDERSON R. M. CASE-FINDING IN PHENYLKETONURIA. I. REPORT OF A SURVEY BY THE COLLEGE OF GENERAL PRACTICE OF CANADA. Can Med Assoc J. 1964 Jun 6;90:1312–1314. [PMC free article] [PubMed] [Google Scholar]
  5. Partington M. W. Case-finding in phenylketonuria: 3. One-way paper chromatography of amino acids in blood. Can Med Assoc J. 1968 Oct 5;99(13):638–644. [PMC free article] [PubMed] [Google Scholar]
  6. Schneider A. J., Garrard S. D. Diagnostic and therapeutic implications of persistent hyperphenylalaninemia in an infant heterozygous for the gene of phenylketonuria. J Pediatr. 1966 May;68(5):704–712. doi: 10.1016/s0022-3476(66)80442-0. [DOI] [PubMed] [Google Scholar]

Articles from Canadian Medical Association Journal are provided here courtesy of Canadian Medical Association

RESOURCES